Clinical QA

San Francisco  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Keywords

Description

This position is responsible for leading the GCP Quality Assurance Audits to assure that all aspects of are executed in compliance with applicable US FDA, ICH GCP Guidelines and other government and/or country specific regulations. This is an exciting mid sized Pharmaceutical company that is thriving and aggresively looking to expand.

Job Requirements:

-Investigate internal GCP Quality issues, initiate process improvements and promote standardization of best practices.

-Assure the integrity and quality of clinical data by independently manage, lead, participate, and follow-up on routine and directed; internal and external; domestic and international GCP audits. Audits will include, but are not limited to: internal systems, investigator study sites, vendors, and study reports.

- Act as a subject matter expert by providing GCP Compliance advice to Clinical Operations and Clinical Development, including updates for applicable regulations.

-Supports the administration of the company's training program, and conduct Good clinical Practice training.

-Travel on a regular basis 30%+

Qualifications:

-5+ years of related experience in the Pharmaceutical/Biotech industry

-Strong knowledge of Code of Federal Regulations and ICG Guidelines governing clinical trials and recent initiatives.

-Excellent verbal and written communication skills and ability to work well in teams

This is an urgent role with open interview slots available asap for the right candidate. Please contact me with your info at b.ross(@)realstaffing.com

To find out more about Real please visit www.realstaffing.com
Start date
04/2013
From
Real Staffing
Published at
06.04.2013
Project ID:
516862
Contract type
Permanent
To apply to this project you must log in.
Register